Canonical Allele Identifier: CA202464525

Gene: GATA3

Linked Data

• dbSNP Id: rs1025677004
• gnomAD v4: 10-8074057-G-T
• MyVariant Identifiers: chr10:g.8116020G>T (hg19) ; chr10:g.8074057G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8074057G>T , CM000672.2:g.8074057G>T	GRCh38
NC_000010.10:g.8116020G>T , CM000672.1:g.8116020G>T	GRCh37
NC_000010.9:g.8156026G>T	NCBI36
NG_015859.1:g.24354G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.*34G>T	ENSP00000341619.3:n.*34G>T
ENST00000379328.9:c.*34G>T MANE Select	ENSP00000368632.3:n.*34G>T
ENST00000346208.3:c.*34G>T	ENSP00000341619.3:n.*34G>T
ENST00000379328.7:c.*34G>T	ENSP00000368632.3:n.*34G>T
ENST00000461472.1:n.888G>T
NM_001002295.1:c.*34G>T	NP_001002295.1:n.*34G>T
NM_002051.2:c.*34G>T	NP_002042.1:n.*34G>T
XM_005252442.2:c.*34G>T	XP_005252499.1:n.*34G>T
XM_005252443.3:c.*34G>T	XP_005252500.1:n.*34G>T
XM_005252443.5:c.*34G>T	XP_005252500.1:n.*34G>T
NM_001002295.2:c.*34G>T MANE Select	NP_001002295.1:n.*34G>T
NM_002051.3:c.*34G>T	NP_002042.1:n.*34G>T